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Dive into the research topics of 'Erratum to: Clinical, biochemical and molecular analysis of 13 Japanese patients with β-ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation (J Inherit Metab Dis, DOI 10.1007/s10545-014-9682-y)'. Together they form a unique fingerprint.- Sort by
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